Summary of Study ST001660
This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001065. The data can be accessed directly via it's Project DOI: 10.21228/M81Q3K This work is supported by NIH grant, U2C- DK119886.
See: https://www.metabolomicsworkbench.org/about/howtocite.php
This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.
Study ID | ST001660 |
Study Title | Plasmodium falciparum metabolomics as a result of treatment with putative acetyl-CoA synthetase inhibitors |
Study Summary | Plasmodium falciparum cells in culture were treated with respective compounds for 2.5 hours at 10xIC50 values. Metabolites were isolated using 90% methanol, dried, reconstituted in HPLC-grade water, and analyzed by HPLC/MS. Resulting data were analyzed and compiled to generate study data. |
Institute | Pennsylvania State University |
Department | Chemistry |
Laboratory | Llinás Laboratory |
Last Name | Llinás |
First Name | Manuel |
Address | W126 Millennium Science Complex, University Park, PENNSYLVANIA, 16802, USA |
mul27@psu.edu | |
Phone | 814-867-3444 |
Submit Date | 2021-01-22 |
Num Groups | 3 |
Total Subjects | 24 |
Raw Data Available | Yes |
Raw Data File Type(s) | mzXML |
Analysis Type Detail | LC-MS |
Release Date | 2021-06-01 |
Release Version | 1 |
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Project:
Project ID: | PR001065 |
Project DOI: | doi: 10.21228/M81Q3K |
Project Title: | Plasmodium falciparum metabolomics as a result of treatment with putative acetyl-CoA synthetase inhibitors |
Project Summary: | Plasmodium falciparum is the most virulent species of parasites that cause malaria. Current drug efforts that are used to combat this deadly disease often employ pharmacologic strategies that inhibit critical parasite metabolic functions. Compounds used in the present study have generated resistance mutations in major acetyl-CoA producing enzymes. Hence, we set out to test the metabolic effects of these compounds on Plasmodium falciparum parasites including those on acetyl-CoA production by treating parasites for 2.5 hours under 10xIC50 of the test compounds. We used a targeted HPLC/mass spectrometry-based approach to analyze parasite metabolism. We find that multiple compounds tested in these studies have led to relative decreases in acetyl-CoA abundance compared to control parasite conditions. These studies are necessary for understanding pharmacology effects on the most virulent human malaria parasite. |
Institute: | Pennsylvania State University |
Department: | Chemistry |
Laboratory: | Llinás Laboratory |
Last Name: | Llinás |
First Name: | Manuel |
Address: | W126 Millennium Science Complex, University Park, PENNSYLVANIA, 16802, USA |
Email: | mul27@psu.edu |
Phone: | 814-867-3444 |
Funding Source: | This work was supported by the Bill and Melinda Gates Foundation (OPP1054480) |